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运动发酵单胞菌磷酸甘油酸激酶基因:克隆、测序及在gap操纵子中的定位

Phosphoglycerate kinase gene from Zymomonas mobilis: cloning, sequencing, and localization within the gap operon.

作者信息

Conway T, Ingram L O

机构信息

Department of Microbiology and Cell Science, University of Florida, Gainesville 32611.

出版信息

J Bacteriol. 1988 Apr;170(4):1926-33. doi: 10.1128/jb.170.4.1926-1933.1988.

Abstract

The Zymomonas mobilis gene encoding phosphoglycerate kinase (EC 2.7.3.2), pgk, has been cloned into Escherichia coli and sequenced. It consists of 336 amino acids, including the N-terminal methionine, with a molecular weight of 41,384. This promoterless gene is located 225 base pairs downstream from the gap gene and is part of the gap operon. Previous studies have shown that the specific activities of glyceraldehyde-3-phosphate dehydrogenase and phosphoglycerate kinase do not change coordinately in Z. mobilis, although the two enzymes appear to be under the control of a common promoter. The translated amino acid sequence for the Z. mobilis phosphoglycerate kinase is less conserved than those of eucaryotic genes. A comparison of known sequences for phosphoglycerate kinase revealed a high degree of conservation of structure with 102 amino acid positions being retained by all. In general, the amino acid positions at the boundaries of beta-sheet and alpha-helical regions and those connecting these regions were more highly conserved than the amino acid positions within regions of secondary structure.

摘要

运动发酵单胞菌中编码磷酸甘油酸激酶(EC 2.7.3.2)的基因pgk已被克隆到大肠杆菌中并进行了测序。它由336个氨基酸组成,包括N端甲硫氨酸,分子量为41384。这个无启动子基因位于gap基因下游225个碱基对处,是gap操纵子的一部分。先前的研究表明,尽管这两种酶似乎受共同启动子的控制,但在运动发酵单胞菌中,3-磷酸甘油醛脱氢酶和磷酸甘油酸激酶的比活性不会协同变化。运动发酵单胞菌磷酸甘油酸激酶的翻译氨基酸序列比真核基因的保守性低。对已知的磷酸甘油酸激酶序列进行比较发现,其结构具有高度保守性,共有102个氨基酸位置保持不变。一般来说,β-折叠和α-螺旋区域边界处以及连接这些区域的氨基酸位置比二级结构区域内的氨基酸位置保守性更高。

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